The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7487529 7913858 I 7487529-7 20101205 20110411 20110518 EXP JP-ASTRAZENECA-2011SE22751 AZPRODUW00 8 YR M Y 20110518 OT JAPAN

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7487529 1016525687 C THP-ADRIAMYCIN 2
7487529 1016525681 PS MEROPENEM 1 INTRAVENOUS 050706
7487529 1016525683 SS MUCODYNE 2 ORAL
7487529 1016525682 SS POLARAMINE 1 ORAL
7487529 1016525684 C FUNGUARD 2
7487529 1016525685 C CYCLOPHOSPHAMIDE 1
7487529 1016525686 C VINCRISTINE SULFATE 1
7487529 1016525688 C CISPLATIN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7487529 1016525687 NEUROBLASTOMA
7487529 1016525681 FEBRILE NEUTROPENIA
7487529 1016525685 NEUROBLASTOMA
7487529 1016525686 NEUROBLASTOMA
7487529 1016525688 NEUROBLASTOMA

Outcome of event

Event ID OUTC COD
7487529 OT

Reactions reported

Event ID PT
7487529 ANAPHYLACTIC REACTION

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7487529 1016525687 20101106
7487529 1016525681 20101201 20101213 13 DAY
7487529 1016525683 20101204
7487529 1016525682 20101204
7487529 1016525684 20101201 20101213 13 DAY
7487529 1016525685 20101106
7487529 1016525686 20101106
7487529 1016525688 20101106